Literature DB >> 15379707

Etoposide: discovery and medicinal chemistry.

Philippe Meresse1, Elsa Dechaux, Claude Monneret, Emmanuel Bertounesque.   

Abstract

Etoposide is an antitumor agent currently in clinical use for the treatment of small cell lung cancer, testicular cancer and lymphomas. Since the introduction of etoposide in 1971, its mechanism of action and potent antineoplastic activity has served as the impetus for intensive research activities in chemistry and biology. This drug acts by stabilizing a normally transient DNA-topoisomerase II complex, thus increasing the concentration of double-stranded DNA breaks. This phenomenon triggers mutagenic and cell death pathways. The function of topoisomerase II is understood in some detail, as is the mechanism of inhibition of etoposide at a molecular level. Etoposide has shortcomings of limited neoplastic activity against several solid tumors such as non-small cell lung cancer, cross-resistance to MDR tumor cell lines and low bioavailability. The design and synthesis of etoposide analogs is an activity of fundamental interest to the field of cancer chemotherapy. In the first part, this article is a survey of the discovery of etoposide, the DNA topoisomerase II structure and mechanism, and the models for drug-enzyme interaction. The last part is concerned with the search for new etoposide analogs based upon an empirical design.

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Year:  2004        PMID: 15379707     DOI: 10.2174/0929867043364531

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  35 in total

1.  Mechanisms of apoptosis are retained in cells with P glycoprotein-mediated drug resistance.

Authors:  A G Paleeva; G E Onishchenko; A A Shtil
Journal:  Dokl Biol Sci       Date:  2006 Mar-Apr

Review 2.  Natural products as leads to anticancer drugs.

Authors:  M Gordaliza
Journal:  Clin Transl Oncol       Date:  2007-12       Impact factor: 3.405

Review 3.  Enantiomeric natural products: occurrence and biogenesis.

Authors:  Jennifer M Finefield; David H Sherman; Martin Kreitman; Robert M Williams
Journal:  Angew Chem Int Ed Engl       Date:  2012-05-03       Impact factor: 15.336

4.  The DNA damage response induces IFN.

Authors:  Sabrina Brzostek-Racine; Chris Gordon; Sarah Van Scoy; Nancy C Reich
Journal:  J Immunol       Date:  2011-10-17       Impact factor: 5.422

5.  Profiling SLCO and SLC22 genes in the NCI-60 cancer cell lines to identify drug uptake transporters.

Authors:  Mitsunori Okabe; Gergely Szakács; Mark A Reimers; Toshihiro Suzuki; Matthew D Hall; Takaaki Abe; John N Weinstein; Michael M Gottesman
Journal:  Mol Cancer Ther       Date:  2008-09       Impact factor: 6.261

6.  5k, a novel β-O-demethyl-epipodophyllotoxin analogue, inhibits the proliferation of cancer cells in vitro and in vivo via the induction of G2 arrest and apoptosis.

Authors:  Danqing Xu; Ji Cao; Shijing Qian; Lin Li; Chunqi Hu; Qinjie Weng; Jianshu Lou; Difeng Zhu; Hong Zhu; Yongzhou Hu; Qiaojun He; Bo Yang
Journal:  Invest New Drugs       Date:  2010-03-30       Impact factor: 3.850

7.  A diazirine-based photoaffinity etoposide probe for labeling topoisomerase II.

Authors:  Gaik-Lean Chee; Jack C Yalowich; Andrew Bodner; Xing Wu; Brian B Hasinoff
Journal:  Bioorg Med Chem       Date:  2009-11-27       Impact factor: 3.641

8.  Loss of putative tumor suppressor EI24/PIG8 confers resistance to etoposide.

Authors:  Christina N Mork; Douglas V Faller; Remco A Spanjaard
Journal:  FEBS Lett       Date:  2007-11-05       Impact factor: 4.124

9.  Embryonic stem cells lacking the epigenetic regulator Cfp1 are hypersensitive to DNA-damaging agents and exhibit decreased Ape1/Ref-1 protein expression and endonuclease activity.

Authors:  Courtney M Tate; Melissa L Fishel; Julianne L Holleran; Merrill J Egorin; David G Skalnik
Journal:  DNA Repair (Amst)       Date:  2009-10-15

Review 10.  Dimeric approaches to anti-cancer chemotherapeutics.

Authors:  M K Hadden; B S J Blagg
Journal:  Anticancer Agents Med Chem       Date:  2008-10       Impact factor: 2.505

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